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Gabapentin as an adjuvant therapy to splinting in carpal tunnel syndrome (CTS): a systematic review and meta-analysis of randomized controlled trials



Carpal tunnel syndrome (CTS) is a common upper limb entrapment neuropathy; severe cases are treated surgically and mild to moderate can be managed conservatively. The purpose of this systematic review and meta-analysis was to define the efficacy of gabapentin as an adjuvant to splinting in the treatment of mild to moderate CTS.


A systematic search through 13 databases, randomized clinical trials (RCTs) reporting the use of gabapentin with splinting in CTS were included and analyzed.


Three RCTs including 170 patients were eligible. There was no significant difference between gabapentin plus splinting and splinting alone in 5 measured parameters: (1) Symptom Severity Scale (SSS) [MD (95% CI) = − 0.76 (− 2.46–0.93), p = 0.378], (2) Functional Status Scale (FSS) [MD (95% CI) = − 0.23 (− 1.40–0.94), p = 0.701], (3) visual analogue scale (VAS) to assess pain [MD (95% CI) = − 0.6 (− 1.47–0.27), p = 0.174], (4) Grip strength [MD (95% CI) = − 0.11 (− 0.70–0.48), p = 0.718], and (5) pinch strength [MD (95% CI) = 0.72 (− 0.10–1.54), p = 0.083].


This review provides low-quality evidence that gabapentin plus nocturnal splinting is not superior to splinting alone. More high-quality trials are needed to determine the role of this drug as an adjuvant in the management of CTS.


Carpal tunnel syndrome (CTS) is a chronic compressive neuropathy resulting from compression of the median nerve at the wrist and considered to be the most common type of upper limb entrapment neuropathy seen in adults in outpatient clinics [1]. It affects 5.3% of women and 2.1% men [2]. It has a prevalence rate of 7.8% and an annual incidence rate of 5.7% in the working population [3].

Although surgical treatment ensures relief of symptoms, it should be only indicated in severe cases with persistent symptoms because of the high cost and possible complications such as infection, nerve injury, tendon injury, and complex regional pain syndrome [4].

Conservative measures are considered as the first-line treatment in mild or moderate cases such as splints, non-steroidal anti-inflammatory drugs, physical therapy, and local steroid injections [5].

Wrist splinting and immobilization in a neutral position is the most popular conservative modality. Oral treatments such as Gabapentin, an antiepileptic drug structurally related to gama-amino butyric acid (GABA), is proposed to be effective for the treatment of neuropathic pain as diabetic neuropathy and post-herpetic neuralgia [6, 7]. According to Hui et al. [8], its benefit as a monotherapy in the management of CTS is limited. Its benefit, however, as an adjuvant to splinting is still controversial [9,10,11].

Therefore, the purpose of this systematic review and meta-analysis was to determine the effectiveness of gabapentin as an adjuvant to splinting versus splinting alone as a conservative line of CTS management.


Search strategy and selection criteria

Two reviewers independently performed an electronic search on 13 databases to retrieve all potentially relevant articles to the research subject. These databases included PubMed, Scopus, Embase, Google Scholar, Cochrane Central Register of Controlled Trials (CENTRAL), International Scientific Indexing (ISI), POPLINE, Global Health Library (GHL), Virtual Health Library (VHL), The New York Academy of Medicine (NYAM), WHO International Clinical Trials Registry Platform (ICTRP),, and System for Information on Grey Literature in Europe (SIGLE). The following search terms were used together searching for all related articles: [gabapentin OR Neurontin OR pregabalin OR Lyrica OR Gaba OR anticonvulsant OR anticonvulsants] AND [(carpal tunnel) OR (entrapment neuropathy) OR (median neuropathy) OR (compression neuropathy) OR CTS]. There was no search filtering applied regarding language, year, and design. Results from scanned databases were grouped into one Endnote library to remove duplications. Two reviewers independently screened titles and abstracts of articles imported into Endnote for eligibility concerning inclusion and exclusion criteria. We included RCTs reporting the use of gabapentin as an adjuvant to splinting as a conservative line of CTS management. Exclusion criteria were (I) study designs other than RCTs, (II) severe cases of CTS required surgical intervention, (III) data cannot be extracted, (IV) overlapped data set, (V) only abstract is available, and (VI) duplication and irrelevant data. A manual search was carried out using references of the included studies, looking for similar articles in PubMed and Google Scholar. Decisions after reviewers’ discussion were further upheld by consulting the senior author. The study selection procedure is summarized in the PRISMA flow diagram (Fig. 1).

Fig. 1
figure 1

PRISMA flow diagram of studies’ screening and selection

Data extraction

Similar to the screening method, two reviewers were responsible for data extraction. A template in Microsoft Excel was used to report baseline characters and inspected outcomes. Further amendments were applied after reviewers’ discussion. All data has been checked by the senior author.

Statistical analysis

All data were analyzed using R statistical software version 3.4.3 [12]. First, mean difference (MD), standardized mean difference (SMD), and associated standard errors (Se) were calculated for the intervention (gabapentin plus splinting) versus control (splinting alone) groups. All data were pooled with the help of “meta” package [13, 14]. A fixed-effect model with the method of Mantel-Haenszel [15] was used when there is no evidence of heterogeneity between studies. Otherwise, a random-effects model with the method of DerSiomonian and Laird was chosen [16]. Heterogeneity between studies was evaluated using the Q statistic and I2 test which describes the percentage of variability in the effect estimates [16, 17].


Literature search and patient characteristics

The electronic search yielded 566 references from the 13 databases. After excluding duplicates and title/abstract screening, we had 24 relevant articles for full-text screening. Only three studies [9,10,11] fulfilled the inclusion criteria, and the manual search of references did not import any additional articles. The eligible three articles included 170 participants (100 intervention and 70 control) collectively, the mean age for intervention and control was 43.8 (SD; 8.1) and 47.18 (SD; 10.7) years, respectively. Patients’ characteristics of each study are summarized in (Table 1). All three studies included only patients with mild to moderate idiopathic CTS. Degree of severity was defined based on clinical findings such as thenar atrophy and EMG findings. The following criteria describe the EMG findings that may be encountered in mild, moderate, and severe cases:

Table 1 Patients’ characteristics of included studies

Mild: median distal sensory peak latency prolongation, either absolute or relative (using sensitive comparative methods) and no evidence of axon loss.

Moderate: abnormal median sensory latency, as noted in the mild type, and absolute or relative prolongation of median motor distal latency (using sensitive comparative methods), and lack of evidence of axon loss.

Severe: any disturbances in nerve conduction studies mentioned above, along with evidence of axon loss, defined as (a) lack or decreased amplitude of sensory nerve action potential or mixed nerve action potential of median nerve, (b) lack of or decreased amplitude of thenar compound muscle action potential, or (c) the presence of fibrillation potentials or changes in motor unit potentials such as increasing amplitude, duration, or phases in needle EMG [18].

Quality assessment of included studies

In order to assess the risk of bias among included RCTs, we used the Cochrane Collaboration’s quality assessment tool [19]. Two reviewers independently carried out the assessment, and dissimilarities were settled by discussing with the senior author. The three included RCTs had a low risk of bias regarding selective reporting and attrition bias. Random sequence generation and allocation concealment were unclear in studies by Eftekharsadat et al. [9] and Mehmetoglu et al. [11] (Fig. 2)

Fig. 2
figure 2

Summary of quality assessment among included RCTs

The included studies evaluated the use of gabapentin plus splinting by observing changes in the following five parameters (clinical and electrophysiological).

Symptom Severity Scale (SSS): pooling of changes in SSS reported by the three studies showed no significant difference between intervention and control groups before and after treatment [MD (95% CI) = − 0.76 (− 2.46–0.93), p = 0.378] (Fig. 3a). A significant heterogeneity was found between studies [I2 = 96%, p < 0.000].

Fig. 3
figure 3

Forest plot meta-analysis comparing changes in in the measured outcomes between gabapentin and control group; (TE = treatment effect, seTE = standard error of treatment effect): a Symptom Severity Scale (SSS), b Functional Severity Scale (FSS), c visual analogue score (VAS), d grip strength, and e pinch strength

Functional Severity Scale (FSS): regarding FSS fluctuations (pre- and post-treatment), results showed no significant difference between intervention and control groups [MD (95% CI) = − 0.23 (− 1.40–0.94), p = 0.701] (Fig. 3b) with significant heterogeneity [I2 = 93%, p < 0.000].

Visual Analogue Score (VAS): monitoring effects of gabapentin using changes in pain assessed by VAS (pre- and post-treatment), there was no significant difference between intervention and control groups [MD (95% CI) = − 0.6 (− 1.47–0.27), p = 0.174] (Fig. 3c) with evidence of heterogeneity [I2 = 87.3%, p < 0.000].

Grip strength: as for the changes in grip strength, no significant difference between intervention and control groups before and after treatment could be detected [MD (95% CI) = − 0.11 (− 0.70–0.48), p = 0.718] (Fig. 3d) A significant heterogeneity was found between studies [I2 = 74.4%, p = 0.009].

Pinch strength: monitoring effects of gabapentin using changes in pinch strength (pre- and post-treatment), there was no significant difference between intervention and control groups [MD (95% CI) = 0.72 (− 0.10–1.54), p = 0.083] (Fig. 3e) with evidence of heterogeneity [I2 = 79.4%, p = 0.008].

Given the high level of heterogeneity in Mehmetoglu et al.’s [11] study in terms of a significant difference in the dose and the follow-up duration compared to the other two studies, a sub-analysis for the studies by Hesami et al. [10] and Eftekharsadat et al. [9] was carried out and the results are demonstrated in (Fig. 4).

Fig. 4
figure 4

Forest plot meta-analysis comparing changes between gabapentin and control group in the sub-group analysis; (TE = treatment effect, seTE = standard error of treatment effect): a Symptom Severity Scale (SSS), b Functional Severity Scale (FSS), c visual analogue score (VAS), and d grip strength


CTS is by far the most common entrapment neuropathy of the upper extremity [20]. While surgery is the treatment of choice in severe cases with evidence of severe nerve affection and cases refractory to conservative therapy [4], splinting with the addition of medications can provide some symptomatic relief in mild to moderate cases; however, controversy still exists regarding the use of Gabapentin as an adjuvant to splining.

In this systematic review and meta-analysis, we studied the benefit of adding Gabapentin to nocturnal splinting in the management of mild and moderate cases of CTS, and we found little evidence to support its effectiveness in improving the functional or electrophysiological outcomes.

Nocturnal splinting is a well-known conservative measure for symptomatic relief of CTS [21, 22]. Its effectiveness had been validated in previous studies [23,24,25]. The rationale behind splinting is that it holds the wrist in the neutral position where the pressure on the median nerve is lowest, thus improving both clinical symptoms and electrophysiological studies [26, 27]. It is an acceptable method for patients in the early phases of CTS, as it is simple, inexpensive, and it can be applied at home [28].

Previous studies have confirmed the effectiveness of gabapentin (1-[amino methyl]-cyclohexane acetic acid; Neurontin, Pfizer) in relieving neuropathic pain syndromes such as trigeminal neuralgia, diabetic neuropathy, reflex sympathetic dystrophy, multiple sclerosis, and post-herpetic neuralgia [29,30,31,32]. A randomized double-blinded placebo-controlled trail by Hui et al. concluded that its use alone in CTS is ineffective [8]. Reports on gabapentin role in CTS were summarized in Table 2 [5, 8, 33,34,35,36]. Since combined therapy is generally superior to monotherapy, other trails were performed to investigate the potential superiority of splinting combined with gabapentin over splinting alone. So, we included these trials in our analysis [9,10,11].

Table 2 Summary of the studies reported on using Gabapentin as a medical line of CTS conservative management

Eftekharsadat et al. [9] studied the effect of a low and high dose of gabapentin and compared their effects to a control group. At the same time, they found a significant improvement achieved by gabapentin regarding SSS, FSS, VAS, grip strength, and pinch strength; they concluded that as the dose of gabapentin increases, so does the effect.

The second study by Hesami et al. [10] showed that gabapentin has no statistically significant effect in mild cases, especially on grip strength but significantly improved the SSS, FSS, VAS, and grip strength in cases with moderate severity.

On the contrary, Mehmetoglu et al. [11] had some contradictory results; they found that the combination of splinting and gabapentin had no superior impact compared to splinting alone except when it comes to the median nerve sensory conduction velocity.

The heterogeneity of the conclusions in these studies can be attributed to the difference in their baseline criteria and the factors associated with the failure of conservative therapy in CTS. Predictors of failure of non-surgical management in CTS include long duration of the symptoms, higher patients’ age, and poor electrodiagnostic studies parameters such as prolonged motor and sensory latencies, and significant evidence of nerve injury.

This can partially explain why Mehmetoglu et al. [11] failed to prove the superiority of the combined treatment over splinting alone as in their study, the patients were older (median age was 47 and 49 years respectively) and the duration of the symptoms was longer (21 and 24 months respectively).

Hesami et al. [10], on the other hand, showed the superiority of the combined treatment in some parameters with a mean age in the gabapentin receiving group of 40 years and the duration of the sensory symptoms was at least 3 months.

Another important difference between these studies was the follow-up duration, while Mehmetoglu et al. [11] had 6 months follow up duration, the other two studies only followed the patients for 1 or 2 months; this may give the impression that gabapentin can improve the symptoms on the short but not on the long term.

The difference in doses was a critical factor as well. Mehmetoglu et al. [11] used 1800 mg, while the other two studies used 100 or 300 mg.

Some adverse effects of gabapentin have been reported in the literature including headache, dizziness, rash, and GIT symptoms causing some patients to abandon the trials [5, 8, 11, 34, 37]. On the other hand, Eftekharsadat et al. [9] used relatively lower doses of gabapentin (100 mg and 300 mg) and did not report any side effects.


There are some limitations to our study. We had to include only three trials with a relatively small, overall and per study, sample size with high type 1 error in the study by Hesami et al. [10]. The studies used different doses of the drug which may have interfered with the effect in each study; the follow-up duration in some studies was not long enough to reflect the long-term effect of gabapentin and they were single-blinded. These drawbacks hindered an analysis with high power or a meta-regression to tackle the clinical heterogeneity between the studies. Although our review is conclusive of the relevant literature, more powerful and well-designed studies are recommended to find evidence of higher quality.


This review suggests no benefit of gabapentin for symptomatic relief or improvement of grip or power strength in patients with mild to moderate CTS. Nevertheless, the low quality of evidence, small sample sizes, and heterogeneity of trial designs prohibit the establishment of a solid conclusion regarding the superiority of gabapentin plus splinting over splinting alone.

Availability of data and materials

The data supporting the results of this article are included within the article.



Carpal tunnel syndrome


Randomized clinical trials


Gama-amino butyric acid


Cochrane Central Register of Controlled Trials (CENTRAL)


International Scientific Indexing


Global Health Library


Virtual Health Library


New York Academy of Medicine


International Clinical Trials Registry Platform


System for Information on Grey Literature in Europe


Mean difference


Standardized mean difference


Standard errors


Standard deviation




Symptom Severity Scale


Functional Severity Scale


Visual analogue score


Confidence interval




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AAK and AMA carried out the study conception and design. AMA and OGH carried out data acquisition. AMA, OGH, and AAK carried out analysis and interpretation of data, drafted the manuscript, and designed the figures. AAK did the critical revision. All authors discussed the results and commented on the manuscript. All authors read and approved the final manuscript.

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Correspondence to Ahmed A. Khalifa.

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Ahmed, A.M., Hassan, O.G. & Khalifa, A.A. Gabapentin as an adjuvant therapy to splinting in carpal tunnel syndrome (CTS): a systematic review and meta-analysis of randomized controlled trials. Egypt J Neurol Psychiatry Neurosurg 56, 104 (2020).

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